1-44401710-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401710
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401710
    reference: chr 1
allele count: 1
allele frequency: 9.345270358671476e-6
allele num: 107006
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.57A>G
  hgvsp: ENST00000438616.3:c.57A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.61-31A>G
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.61-55A>G
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.61-55A>G
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.61-31A>G
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.61-55A>G
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.61-31A>G
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.61-31A>G
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.61-55A>G
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.61-31A>G
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.61-31A>G
  variant of: http://identifiers.org/hgnc/727
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6546
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln19Gln
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

1-44401716-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401716
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401716
    reference: chr 1
allele count: 1
allele frequency: 9.168760200245722e-6
allele num: 109066
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.61-25C>G
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.61-49C>G
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.63C>G
  hgvsp: ENSP00000391998.3:p.His21Gln
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.61-49C>G
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.61-49C>G
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.61-25C>G
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.61-49C>G
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.61-25C>G
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.61-25C>G
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.61-25C>G
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.61-25C>G
  variant of: http://identifiers.org/hgnc/727
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 7.25e1
  variant carriers: 0
hgvs: p.His21Gln
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum

1-44401723-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401723
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401723
    reference: chr 1
allele count: 1
allele frequency: 9.044208089139715e-6
allele num: 110568
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.61-18G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.61-18G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.70G>A
  hgvsp: ENSP00000391998.3:p.Ala24Thr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.61-18G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.61-42G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.61-42G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.61-42G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.61-18G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.61-42G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.61-18G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.61-18G>A
  variant of: http://identifiers.org/hgnc/727
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4805
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala24Thr
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

1-44401727-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401727
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401727
    reference: chr 1
allele count: 3
allele frequency: 2.703969427119011e-5
allele num: 110948
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.74T>C
  hgvsp: ENSP00000391998.3:p.Leu25Pro
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.61-38T>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.61-14T>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.61-38T>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.61-14T>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.61-38T>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.61-38T>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.61-14T>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.61-14T>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.61-14T>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.61-14T>C
  variant of: http://identifiers.org/hgnc/727
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39457
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11428
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu25Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

1-44401728-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401728
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401728
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 111120
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.61-37C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.61-37C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.61-37C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.61-13C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.61-13C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.61-13C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.61-13C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.61-13C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.75C>T
  hgvsp: ENST00000438616.3:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.61-13C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.61-37C>T
  variant of: http://identifiers.org/hgnc/727
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4565
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu25Leu
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

1-44401736-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401736
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401736
    reference: chr 1
allele count: 3
allele frequency: 2.684755955683628e-5
allele num: 111742
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.83C>T
  hgvsp: ENSP00000391998.3:p.Pro28Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.61-29C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.61-5C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.61-29C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.61-5C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.61-5C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.61-29C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.61-5C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.61-5C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.61-5C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.61-29C>T
  variant of: http://identifiers.org/hgnc/727
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11736
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro28Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

1-44401742-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401742
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401742
    reference: chr 1
allele count: 1
allele frequency: 8.937828465196096e-6
allele num: 111884
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.62C>T
  hgvsp: ENSP00000436149.1:p.Ala21Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.89C>T
  hgvsp: ENSP00000391998.3:p.Ala30Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.62C>T
  hgvsp: ENSP00000436727.1:p.Ala21Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.61-23C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.62C>T
  hgvsp: ENSP00000387435.3:p.Ala21Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.62C>T
  hgvsp: ENSP00000434071.1:p.Ala21Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.61-23C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.61-23C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.62C>T
  hgvsp: ENSP00000434856.1:p.Ala21Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.62C>T
  hgvsp: ENSP00000435140.1:p.Ala21Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.61-23C>T
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39235
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11876
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala21Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

1-44401747-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401747
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401747
    reference: chr 1
allele count: 5
allele frequency: 4.476836846157979e-5
allele num: 111686
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.67C>T
  hgvsp: ENSP00000436149.1:p.Leu23Phe
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.67C>T
  hgvsp: ENSP00000435140.1:p.Leu23Phe
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.61-18C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.67C>T
  hgvsp: ENSP00000436727.1:p.Leu23Phe
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.67C>T
  hgvsp: ENSP00000434071.1:p.Leu23Phe
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.94C>T
  hgvsp: ENSP00000391998.3:p.Leu32Phe
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.61-18C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.67C>T
  hgvsp: ENSP00000387435.3:p.Leu23Phe
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.61-18C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.67C>T
  hgvsp: ENSP00000434856.1:p.Leu23Phe
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.61-18C>T
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu23Phe
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

1-44401751-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401751
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401751
    reference: chr 1
allele count: 1
allele frequency: 8.985371814685692e-6
allele num: 111292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.71G>A
  hgvsp: ENSP00000436727.1:p.Gly24Asp
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.71G>A
  hgvsp: ENSP00000435140.1:p.Gly24Asp
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.71G>A
  hgvsp: ENSP00000434071.1:p.Gly24Asp
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.71G>A
  hgvsp: ENSP00000436149.1:p.Gly24Asp
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.61-14G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.71G>A
  hgvsp: ENSP00000434856.1:p.Gly24Asp
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.61-14G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.61-14G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.71G>A
  hgvsp: ENSP00000387435.3:p.Gly24Asp
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.98G>A
  hgvsp: ENSP00000391998.3:p.Gly33Asp
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.61-14G>A
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly24Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

1-44401758-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401758
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401758
    reference: chr 1
allele count: 2
allele frequency: 1.807272464396732e-5
allele num: 110664
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.78C>T
  hgvsp: ENST00000498139.2:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.61-7C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.78C>T
  hgvsp: ENST00000474592.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.61-7C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.61-7C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.78C>T
  hgvsp: ENST00000472435.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.78C>T
  hgvsp: ENST00000414809.3:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.61-7C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.78C>T
  hgvsp: ENST00000491846.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.105C>T
  hgvsp: ENST00000438616.3:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.78C>T
  hgvsp: ENST00000479128.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11728
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37732
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.61-7C>T
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD

1-44401760-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401760
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401760
    reference: chr 1
allele count: 2
allele frequency: 1.81123326873268e-5
allele num: 110422
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.80C>T
  hgvsp: ENSP00000435140.1:p.Ala27Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.61-5C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.80C>T
  hgvsp: ENSP00000436149.1:p.Ala27Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.80C>T
  hgvsp: ENSP00000434071.1:p.Ala27Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.80C>T
  hgvsp: ENSP00000436727.1:p.Ala27Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.80C>T
  hgvsp: ENSP00000434856.1:p.Ala27Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.61-5C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.107C>T
  hgvsp: ENSP00000391998.3:p.Ala36Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.61-5C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.80C>T
  hgvsp: ENSP00000387435.3:p.Ala27Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.61-5C>T
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11742
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala27Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

1-44401767-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401767
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401767
    reference: chr 1
allele count: 1
allele frequency: 9.157006025309965e-6
allele num: 109206
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.87T>C
  hgvsp: ENST00000474592.1:c.87T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.87T>C
  hgvsp: ENST00000414809.3:c.87T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.87T>C
  hgvsp: ENST00000491846.1:c.87T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.87T>C
  hgvsp: ENST00000472435.1:c.87T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.87T>C
  hgvsp: ENST00000479128.1:c.87T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.114T>C
  hgvsp: ENST00000438616.3:c.114T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.63T>C
  hgvsp: ENST00000372354.3:c.63T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.63T>C
  hgvsp: ENST00000477048.1:c.63T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.63T>C
  hgvsp: ENST00000372359.5:c.63T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.63T>C
  hgvsp: ENST00000471394.2:c.63T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.87T>C
  hgvsp: ENST00000498139.2:c.87T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11703
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.63T>C
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD

1-44401768-G-GCCCTGTGGCCCA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401768
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401780
    reference: chr 1
allele count: 1
allele frequency: 9.215400777779826e-6
allele num: 108514
alternate allele: GCCCTGTGGCCCA
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsp: ENSP00000387435.3:p.Trp32_Leu35dup
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsp: ENSP00000435804.1:p.Trp24_Leu27dup
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsp: ENSP00000391998.3:p.Trp41_Leu44dup
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsp: ENSP00000435140.1:p.Trp32_Leu35dup
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsp: ENSP00000436149.1:p.Trp32_Leu35dup
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsp: ENSP00000434784.1:p.Trp24_Leu27dup
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsp: ENSP00000436727.1:p.Trp32_Leu35dup
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsp: ENSP00000434856.1:p.Trp32_Leu35dup
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsp: ENSP00000361434.5:p.Trp24_Leu27dup
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsp: ENSP00000434071.1:p.Trp32_Leu35dup
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsp: ENSP00000361429.3:p.Trp24_Leu27dup
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: inframe insertion
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5495
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4179
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Trp32_Leu35dup
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

1-44401775-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401775
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401775
    reference: chr 1
allele count: 1
allele frequency: 9.495233392836797e-6
allele num: 105316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.122G>T
  hgvsp: ENSP00000391998.3:p.Trp41Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.95G>T
  hgvsp: ENSP00000434856.1:p.Trp32Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.95G>T
  hgvsp: ENSP00000436727.1:p.Trp32Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.71G>T
  hgvsp: ENSP00000435804.1:p.Trp24Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.71G>T
  hgvsp: ENSP00000434784.1:p.Trp24Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.95G>T
  hgvsp: ENSP00000436149.1:p.Trp32Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.71G>T
  hgvsp: ENSP00000361434.5:p.Trp24Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.95G>T
  hgvsp: ENSP00000435140.1:p.Trp32Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.95G>T
  hgvsp: ENSP00000387435.3:p.Trp32Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.71G>T
  hgvsp: ENSP00000361429.3:p.Trp24Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.95G>T
  hgvsp: ENSP00000434071.1:p.Trp32Leu
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6730
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6062
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32418
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp32Leu
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

1-44401781-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401781
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401781
    reference: chr 1
allele count: 43
allele frequency: 4.109562857197469e-4
allele num: 104634
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.101C>T
  hgvsp: ENSP00000387435.3:p.Thr34Ile
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.128C>T
  hgvsp: ENSP00000391998.3:p.Thr43Ile
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.101C>T
  hgvsp: ENSP00000434071.1:p.Thr34Ile
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.77C>T
  hgvsp: ENSP00000361434.5:p.Thr26Ile
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.101C>T
  hgvsp: ENSP00000434856.1:p.Thr34Ile
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.101C>T
  hgvsp: ENSP00000436149.1:p.Thr34Ile
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.77C>T
  hgvsp: ENSP00000435804.1:p.Thr26Ile
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.77C>T
  hgvsp: ENSP00000434784.1:p.Thr26Ile
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.101C>T
  hgvsp: ENSP00000436727.1:p.Thr34Ile
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.101C>T
  hgvsp: ENSP00000435140.1:p.Thr34Ile
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.77C>T
  hgvsp: ENSP00000361429.3:p.Thr26Ile
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 11040
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 6430
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7080
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31774
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr34Ile
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS

1-44401785-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401785
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401785
    reference: chr 1
allele count: 1
allele frequency: 9.77326035965598e-6
allele num: 102320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.81G>A
  hgvsp: ENST00000372359.5:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.81G>A
  hgvsp: ENST00000372354.3:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.105G>A
  hgvsp: ENST00000474592.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.105G>A
  hgvsp: ENST00000491846.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.81G>A
  hgvsp: ENST00000471394.2:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.105G>A
  hgvsp: ENST00000479128.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.132G>A
  hgvsp: ENST00000438616.3:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.105G>A
  hgvsp: ENST00000414809.3:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.81G>A
  hgvsp: ENST00000477048.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.105G>A
  hgvsp: ENST00000498139.2:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.105G>A
  hgvsp: ENST00000472435.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7814
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10379
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7953
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu35Leu
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

1-44401788-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401788
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401788
    reference: chr 1
allele count: 11
allele frequency: 1.08476983156483e-4
allele num: 101404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.84C>T
  hgvsp: ENST00000372354.3:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.84C>T
  hgvsp: ENST00000471394.2:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.108C>T
  hgvsp: ENST00000498139.2:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.84C>T
  hgvsp: ENST00000372359.5:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.108C>T
  hgvsp: ENST00000491846.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.108C>T
  hgvsp: ENST00000472435.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.108C>T
  hgvsp: ENST00000474592.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.108C>T
  hgvsp: ENST00000479128.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.84C>T
  hgvsp: ENST00000477048.1:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.135C>T
  hgvsp: ENST00000438616.3:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.108C>T
  hgvsp: ENST00000414809.3:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8359
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29225
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10046
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala36Ala
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

1-44401795-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401795
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401795
    reference: chr 1
allele count: 1
allele frequency: 1.030226855953681e-5
allele num: 97066
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.91G>T
  hgvsp: ENSP00000434784.1:p.Ala31Ser
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.115G>T
  hgvsp: ENSP00000435140.1:p.Ala39Ser
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.91G>T
  hgvsp: ENSP00000361434.5:p.Ala31Ser
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.142G>T
  hgvsp: ENSP00000391998.3:p.Ala48Ser
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.115G>T
  hgvsp: ENSP00000436727.1:p.Ala39Ser
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.91G>T
  hgvsp: ENSP00000435804.1:p.Ala31Ser
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.115G>T
  hgvsp: ENSP00000434856.1:p.Ala39Ser
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.115G>T
  hgvsp: ENSP00000434071.1:p.Ala39Ser
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.115G>T
  hgvsp: ENSP00000387435.3:p.Ala39Ser
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.91G>T
  hgvsp: ENSP00000361429.3:p.Ala31Ser
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.115G>T
  hgvsp: ENSP00000436149.1:p.Ala39Ser
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9927
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25243
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala39Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

1-44401809-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401809
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401809
    reference: chr 1
allele count: 1
allele frequency: 1.194914444125801e-5
allele num: 83688
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.105C>T
  hgvsp: ENST00000471394.2:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.129C>T
  hgvsp: ENST00000414809.3:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.129C>T
  hgvsp: ENST00000498139.2:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.129C>T
  hgvsp: ENST00000479128.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.156C>T
  hgvsp: ENST00000438616.3:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.105C>T
  hgvsp: ENST00000372359.5:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.129C>T
  hgvsp: ENST00000474592.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.129C>T
  hgvsp: ENST00000472435.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.105C>T
  hgvsp: ENST00000372354.3:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.105C>T
  hgvsp: ENST00000477048.1:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.129C>T
  hgvsp: ENST00000491846.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14578
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5277
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser43Ser
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

1-44401810-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401810
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401810
    reference: chr 1
allele count: 1
allele frequency: 1.214004758898655e-5
allele num: 82372
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.157G>C
  hgvsp: ENSP00000391998.3:p.Val53Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.106G>C
  hgvsp: ENSP00000361434.5:p.Val36Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.106G>C
  hgvsp: ENSP00000361429.3:p.Val36Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.130G>C
  hgvsp: ENSP00000387435.3:p.Val44Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.106G>C
  hgvsp: ENSP00000435804.1:p.Val36Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.130G>C
  hgvsp: ENSP00000434071.1:p.Val44Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.106G>C
  hgvsp: ENSP00000434784.1:p.Val36Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.130G>C
  hgvsp: ENSP00000436727.1:p.Val44Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.130G>C
  hgvsp: ENSP00000436149.1:p.Val44Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.130G>C
  hgvsp: ENSP00000434856.1:p.Val44Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.130G>C
  hgvsp: ENSP00000435140.1:p.Val44Leu
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4981
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19886
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3565
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14934
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12529
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val44Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

1-44401811-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401811
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401811
    reference: chr 1
allele count: 6
allele frequency: 7.346099221313482e-5
allele num: 81676
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.131T>C
  hgvsp: ENSP00000387435.3:p.Val44Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.131T>C
  hgvsp: ENSP00000436727.1:p.Val44Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.131T>C
  hgvsp: ENSP00000434856.1:p.Val44Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.107T>C
  hgvsp: ENSP00000361434.5:p.Val36Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.131T>C
  hgvsp: ENSP00000436149.1:p.Val44Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.131T>C
  hgvsp: ENSP00000435140.1:p.Val44Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.158T>C
  hgvsp: ENSP00000391998.3:p.Val53Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.107T>C
  hgvsp: ENSP00000435804.1:p.Val36Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.107T>C
  hgvsp: ENSP00000434784.1:p.Val36Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.107T>C
  hgvsp: ENSP00000361429.3:p.Val36Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.131T>C
  hgvsp: ENSP00000434071.1:p.Val44Ala
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4718
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11880
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 20341
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15198
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val44Ala
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

1-44401814-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401814
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401814
    reference: chr 1
allele count: 2
allele frequency: 2.590136759220887e-5
allele num: 77216
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.134C>T
  hgvsp: ENSP00000436149.1:p.Ala45Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.134C>T
  hgvsp: ENSP00000434071.1:p.Ala45Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.110C>T
  hgvsp: ENSP00000361429.3:p.Ala37Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.134C>T
  hgvsp: ENSP00000434856.1:p.Ala45Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.161C>T
  hgvsp: ENSP00000391998.3:p.Ala54Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.110C>T
  hgvsp: ENSP00000361434.5:p.Ala37Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.110C>T
  hgvsp: ENSP00000435804.1:p.Ala37Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.134C>T
  hgvsp: ENSP00000436727.1:p.Ala45Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.134C>T
  hgvsp: ENSP00000435140.1:p.Ala45Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.110C>T
  hgvsp: ENSP00000434784.1:p.Ala37Val
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.134C>T
  hgvsp: ENSP00000387435.3:p.Ala45Val
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16099
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9211
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21855
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala45Val
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-44401817-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401817
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401817
    reference: chr 1
allele count: 1
allele frequency: 1.336969891438045e-5
allele num: 74796
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.137A>G
  hgvsp: ENSP00000436149.1:p.Glu46Gly
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.137A>G
  hgvsp: ENSP00000435140.1:p.Glu46Gly
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.113A>G
  hgvsp: ENSP00000435804.1:p.Glu38Gly
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.137A>G
  hgvsp: ENSP00000387435.3:p.Glu46Gly
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.113A>G
  hgvsp: ENSP00000361434.5:p.Glu38Gly
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.137A>G
  hgvsp: ENSP00000434856.1:p.Glu46Gly
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.137A>G
  hgvsp: ENSP00000434071.1:p.Glu46Gly
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.137A>G
  hgvsp: ENSP00000436727.1:p.Glu46Gly
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.164A>G
  hgvsp: ENSP00000391998.3:p.Glu55Gly
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.113A>G
  hgvsp: ENSP00000434784.1:p.Glu38Gly
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.113A>G
  hgvsp: ENSP00000361429.3:p.Glu38Gly
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16455
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu46Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

1-44401821-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401821
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401821
    reference: chr 1
allele count: 41
allele frequency: 6.404648837790552e-4
allele num: 64016
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.141C>T
  hgvsp: ENST00000491846.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.117C>T
  hgvsp: ENST00000372359.5:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.141C>T
  hgvsp: ENST00000479128.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.117C>T
  hgvsp: ENST00000477048.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.141C>T
  hgvsp: ENST00000414809.3:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.117C>T
  hgvsp: ENST00000471394.2:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.141C>T
  hgvsp: ENST00000474592.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.141C>T
  hgvsp: ENST00000472435.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.117C>T
  hgvsp: ENST00000372354.3:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.141C>T
  hgvsp: ENST00000498139.2:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.168C>T
  hgvsp: ENST00000438616.3:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 1.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8910
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17256
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala47Ala
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

1-44401833-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401833
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401833
    reference: chr 1
allele count: 1
allele frequency: 2.105351804286496e-5
allele num: 47498
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.153C>T
  hgvsp: ENST00000491846.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.153C>T
  hgvsp: ENST00000472435.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.153C>T
  hgvsp: ENST00000479128.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.180C>T
  hgvsp: ENST00000438616.3:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.153C>T
  hgvsp: ENST00000474592.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.129C>T
  hgvsp: ENST00000477048.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.129C>T
  hgvsp: ENST00000372354.3:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.153C>T
  hgvsp: ENST00000414809.3:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.129C>T
  hgvsp: ENST00000372359.5:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.153C>T
  hgvsp: ENST00000498139.2:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.129C>T
  hgvsp: ENST00000471394.2:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17279
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14952
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18640
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser51Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

1-44401851-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401851
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401851
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 21518
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.147C>T
  hgvsp: ENST00000471394.2:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.147C>T
  hgvsp: ENST00000477048.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.171C>T
  hgvsp: ENST00000474592.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.171C>T
  hgvsp: ENST00000491846.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.171C>T
  hgvsp: ENST00000472435.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.171C>T
  hgvsp: ENST00000479128.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.147C>T
  hgvsp: ENST00000372354.3:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.198C>T
  hgvsp: ENST00000438616.3:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.147C>T
  hgvsp: ENST00000372359.5:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.171C>T
  hgvsp: ENST00000414809.3:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.171C>T
  hgvsp: ENST00000498139.2:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16673
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25424
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala57Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP

1-44401853-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401853
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401853
    reference: chr 1
allele count: 1
allele frequency: 6.173601679219657e-5
allele num: 16198
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.173C>G
  hgvsp: ENSP00000434071.1:p.Pro58Arg
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.173C>G
  hgvsp: ENSP00000435140.1:p.Pro58Arg
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.149C>G
  hgvsp: ENSP00000434784.1:p.Pro50Arg
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.149C>G
  hgvsp: ENSP00000435804.1:p.Pro50Arg
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.173C>G
  hgvsp: ENSP00000436149.1:p.Pro58Arg
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.173C>G
  hgvsp: ENSP00000436727.1:p.Pro58Arg
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.173C>G
  hgvsp: ENSP00000387435.3:p.Pro58Arg
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.149C>G
  hgvsp: ENSP00000361429.3:p.Pro50Arg
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.149C>G
  hgvsp: ENSP00000361434.5:p.Pro50Arg
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.200C>G
  hgvsp: ENSP00000391998.3:p.Pro67Arg
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.173C>G
  hgvsp: ENSP00000434856.1:p.Pro58Arg
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26657
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15518
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro58Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

1-44401862-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401862
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401862
    reference: chr 1
allele count: 13
allele frequency: 1.422630772597943e-3
allele num: 9138
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.182G>C
  hgvsp: ENSP00000387435.3:p.Gly61Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.182G>C
  hgvsp: ENSP00000436727.1:p.Gly61Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.158G>C
  hgvsp: ENSP00000434784.1:p.Gly53Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.158G>C
  hgvsp: ENSP00000361434.5:p.Gly53Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.182G>C
  hgvsp: ENSP00000434071.1:p.Gly61Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.182G>C
  hgvsp: ENSP00000435140.1:p.Gly61Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.209G>C
  hgvsp: ENSP00000391998.3:p.Gly70Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.158G>C
  hgvsp: ENSP00000361429.3:p.Gly53Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.182G>C
  hgvsp: ENSP00000434856.1:p.Gly61Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.158G>C
  hgvsp: ENSP00000435804.1:p.Gly53Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.182G>C
  hgvsp: ENSP00000436149.1:p.Gly61Ala
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13571
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27667
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3713
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly61Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/1-44401863-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401863
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401863
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 11454
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.159C>A
  hgvsp: ENST00000471394.2:c.159C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.159C>A
  hgvsp: ENST00000477048.1:c.159C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.183C>A
  hgvsp: ENST00000498139.2:c.183C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.183C>A
  hgvsp: ENST00000491846.1:c.183C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.183C>A
  hgvsp: ENST00000472435.1:c.183C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.183C>A
  hgvsp: ENST00000414809.3:c.183C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.159C>A
  hgvsp: ENST00000372359.5:c.159C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.183C>A
  hgvsp: ENST00000479128.1:c.183C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.159C>A
  hgvsp: ENST00000372354.3:c.159C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.210C>A
  hgvsp: ENST00000438616.3:c.210C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.183C>A
  hgvsp: ENST00000474592.1:c.183C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 29013
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3659
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12383
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly61Gly
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

1-44401886-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401886
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401886
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 5478
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.206C>T
  hgvsp: ENSP00000387435.3:p.Pro69Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.182C>T
  hgvsp: ENSP00000435804.1:p.Pro61Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.206C>T
  hgvsp: ENSP00000436149.1:p.Pro69Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.182C>T
  hgvsp: ENSP00000434784.1:p.Pro61Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.233C>T
  hgvsp: ENSP00000391998.3:p.Pro78Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.206C>T
  hgvsp: ENSP00000436727.1:p.Pro69Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.206C>T
  hgvsp: ENSP00000434856.1:p.Pro69Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.206C>T
  hgvsp: ENSP00000434071.1:p.Pro69Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.182C>T
  hgvsp: ENSP00000361434.5:p.Pro61Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.182C>T
  hgvsp: ENSP00000361429.3:p.Pro61Leu
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.206C>T
  hgvsp: ENSP00000435140.1:p.Pro69Leu
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27473
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6961
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro69Leu
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/1-44401890-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401890
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401890
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 4710
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.186C>A
  hgvsp: ENST00000372354.3:c.186C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.237C>A
  hgvsp: ENST00000438616.3:c.237C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.210C>A
  hgvsp: ENST00000472435.1:c.210C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.210C>A
  hgvsp: ENST00000491846.1:c.210C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.210C>A
  hgvsp: ENST00000414809.3:c.210C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.210C>A
  hgvsp: ENST00000479128.1:c.210C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.186C>A
  hgvsp: ENST00000372359.5:c.186C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435804
  ensembl transcript: ENST00000471394
  gene symbol: ARTN
  hgvsc: ENST00000471394.2:c.186C>A
  hgvsp: ENST00000471394.2:c.186C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434784
  ensembl transcript: ENST00000477048
  gene symbol: ARTN
  hgvsc: ENST00000477048.1:c.186C>A
  hgvsp: ENST00000477048.1:c.186C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.210C>A
  hgvsp: ENST00000474592.1:c.210C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.210C>A
  hgvsp: ENST00000498139.2:c.210C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6256
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27422
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala70Ala
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

1-44401923-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401923
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401923
    reference: chr 1
allele count: 1
allele frequency: 2.145922746781116e-3
allele num: 466
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.199+20G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.*12G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.223+20G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.*12G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.223+20G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.223+20G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.250+20G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.199+20G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.223+20G>A
  variant of: http://identifiers.org/hgnc/727
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18455
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 709
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15439
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/1-44401930-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401930
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401930
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 280
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.223+27C>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.199+27C>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.223+27C>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.*19C>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.223+27C>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.223+27C>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.199+27C>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.250+27C>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.*19C>A
  variant of: http://identifiers.org/hgnc/727
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18042
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3052
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD

1-44401943-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401943
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401943
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 102
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.251-31G>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.224-31G>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.200-31G>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.224-31G>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.*32G>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.*32G>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.200-31G>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.224-31G>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.224-31G>C
  variant of: http://identifiers.org/hgnc/727
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16849
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1987
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

1-44401944-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401944
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401944
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 90
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.200-30G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.*33G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.*33G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.224-30G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.200-30G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.251-30G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.224-30G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.224-30G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.224-30G>A
  variant of: http://identifiers.org/hgnc/727
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16719
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

1-44401952-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401952
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401952
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 74
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.*41G>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.224-22G>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.*41G>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.224-22G>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.224-22G>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.224-22G>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.200-22G>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.200-22G>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.251-22G>C
  variant of: http://identifiers.org/hgnc/727
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16250
  bin: 2.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1592
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-44401966-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401966
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401966
    reference: chr 1
allele count: 11
allele frequency: 1.222222222222222e-1
allele num: 90
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.251-8C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.*55C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.224-8C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.224-8C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.224-8C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.200-8C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.224-8C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.200-8C>T
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.*55C>T
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 7.5e0
  variant carriers: 122
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14570
  bin: 2.5e0
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.25e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 6.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 8.25e1
  variant carriers: 4
hgvs: c.224-8C>T
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

1-44401989-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401989
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401989
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 64
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.239G>A
  hgvsp: ENSP00000387435.3:p.Arg80His
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.*78G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.215G>A
  hgvsp: ENSP00000361434.5:p.Arg72His
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.266G>A
  hgvsp: ENSP00000391998.3:p.Arg89His
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.*78G>A
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.239G>A
  hgvsp: ENSP00000436149.1:p.Arg80His
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.215G>A
  hgvsp: ENSP00000361429.3:p.Arg72His
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.239G>A
  hgvsp: ENSP00000434856.1:p.Arg80His
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.239G>A
  hgvsp: ENSP00000436727.1:p.Arg80His
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11347
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg80His
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

1-44401998-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44401998
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44401998
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 68
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.275G>C
  hgvsp: ENSP00000391998.3:p.Ser92Thr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.248G>C
  hgvsp: ENSP00000387435.3:p.Ser83Thr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434071
  ensembl transcript: ENST00000479128
  gene symbol: ARTN
  hgvsc: ENST00000479128.1:c.*87G>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000434856
  ensembl transcript: ENST00000474592
  gene symbol: ARTN
  hgvsc: ENST00000474592.1:c.248G>C
  hgvsp: ENSP00000434856.1:p.Ser83Thr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000435140
  ensembl transcript: ENST00000472435
  gene symbol: ARTN
  hgvsc: ENST00000472435.1:c.*87G>C
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.248G>C
  hgvsp: ENSP00000436727.1:p.Ser83Thr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.224G>C
  hgvsp: ENSP00000361434.5:p.Ser75Thr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436149
  ensembl transcript: ENST00000491846
  gene symbol: ARTN
  hgvsc: ENST00000491846.1:c.248G>C
  hgvsp: ENSP00000436149.1:p.Ser83Thr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.224G>C
  hgvsp: ENSP00000361429.3:p.Ser75Thr
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser83Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

1-44402031-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402031
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402031
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 44
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.257C>G
  hgvsp: ENSP00000361434.5:p.Ser86Cys
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.281C>G
  hgvsp: ENSP00000436727.1:p.Ser94Cys
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.257C>G
  hgvsp: ENSP00000361429.3:p.Ser86Cys
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.281C>G
  hgvsp: ENSP00000387435.3:p.Ser94Cys
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.308C>G
  hgvsp: ENSP00000391998.3:p.Ser103Cys
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5336
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5252
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser94Cys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD

1-44402147-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402147
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402147
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 36
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.397C>T
  hgvsp: ENST00000498139.2:c.397C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.397C>T
  hgvsp: ENST00000414809.3:c.397C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.373C>T
  hgvsp: ENST00000372359.5:c.373C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.373C>T
  hgvsp: ENST00000372354.3:c.373C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.424C>T
  hgvsp: ENST00000438616.3:c.424C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6079
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5954
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
hgvs: p.Leu133Leu
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

1-44402193-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402193
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402193
    reference: chr 1
allele count: 3
allele frequency: 4.793863854266539e-4
allele num: 6258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.443G>A
  hgvsp: ENSP00000436727.1:p.Arg148His
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.443G>A
  hgvsp: ENSP00000387435.3:p.Arg148His
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.419G>A
  hgvsp: ENSP00000361434.5:p.Arg140His
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.470G>A
  hgvsp: ENSP00000391998.3:p.Arg157His
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.419G>A
  hgvsp: ENSP00000361429.3:p.Arg140His
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32575
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6054
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5364
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2469
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31606
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg148His
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

1-44402197-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402197
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402197
    reference: chr 1
allele count: 1
allele frequency: 1.391207568169171e-4
allele num: 7188
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.423C>T
  hgvsp: ENST00000372359.5:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.474C>T
  hgvsp: ENST00000438616.3:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.447C>T
  hgvsp: ENST00000414809.3:c.447C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.447C>T
  hgvsp: ENST00000498139.2:c.447C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.423C>T
  hgvsp: ENST00000372354.3:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33260
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6541
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32416
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2906
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser149Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

1-44402203-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402203
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402203
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 8512
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.453G>C
  hgvsp: ENSP00000436727.1:p.Glu151Asp
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.453G>C
  hgvsp: ENSP00000387435.3:p.Glu151Asp
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.480G>C
  hgvsp: ENSP00000391998.3:p.Glu160Asp
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.429G>C
  hgvsp: ENSP00000361434.5:p.Glu143Asp
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.429G>C
  hgvsp: ENSP00000361429.3:p.Glu143Asp
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32754
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10057
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9225
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3539
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu151Asp
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD

1-44402214-T-TCCGCTTCTGCAG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402214
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402226
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 10328
alternate allele: TCCGCTTCTGCAG
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsp: ENSP00000361429.3:p.Arg148_Ser151dup
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsp: ENSP00000387435.3:p.Arg156_Ser159dup
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsp: ENSP00000436727.1:p.Arg156_Ser159dup
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsp: ENSP00000361434.5:p.Arg148_Ser151dup
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsp: ENSP00000391998.3:p.Arg165_Ser168dup
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: inframe insertion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15983
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29017
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14411
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1099
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28180
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg156_Ser159dup
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

1-44402239-CCG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402239
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402237
    reference: chr 1
allele count: 1
allele frequency: 5.308419152776303e-5
allele num: 18838
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.497_498delGC
  hgvsp: ENSP00000436727.1:p.Arg166LeufsTer90
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.497_498delGC
  hgvsp: ENSP00000387435.3:p.Arg166LeufsTer90
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.473_474delGC
  hgvsp: ENSP00000361429.3:p.Arg158LeufsTer?
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.524_525delGC
  hgvsp: ENSP00000391998.3:p.Arg175LeufsTer?
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.473_474delGC
  hgvsp: ENSP00000361434.5:p.Arg158LeufsTer90
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16268
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27545
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15646
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26312
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1076
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg166LeufsTer90
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: CCG
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

1-44402251-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402251
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402251
    reference: chr 1
allele count: 4
allele frequency: 1.529753709652746e-4
allele num: 26148
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.477T>G
  hgvsp: ENST00000372359.5:c.477T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.477T>G
  hgvsp: ENST00000372354.3:c.477T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.528T>G
  hgvsp: ENST00000438616.3:c.528T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.501T>G
  hgvsp: ENST00000498139.2:c.501T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.501T>G
  hgvsp: ENST00000414809.3:c.501T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29961
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 899
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11774
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9070
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29340
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.75e1
  variant carriers: 3
hgvs: p.Ser167Ser
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD

1-44402251-TCC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402251
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402249
    reference: chr 1
allele count: 1
allele frequency: 3.824384274131865e-5
allele num: 26148
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.478_479delCC
  hgvsp: ENSP00000361434.5:p.Pro160ThrfsTer88
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.478_479delCC
  hgvsp: ENSP00000361429.3:p.Pro160ThrfsTer?
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.502_503delCC
  hgvsp: ENSP00000436727.1:p.Pro168ThrfsTer88
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.529_530delCC
  hgvsp: ENSP00000391998.3:p.Pro177ThrfsTer?
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.502_503delCC
  hgvsp: ENSP00000387435.3:p.Pro168ThrfsTer88
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29961
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9070
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11774
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 899
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29340
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro168ThrfsTer88
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: TCC
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-44402253-C-CGGAG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402253
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402257
    reference: chr 1
allele count: 1
allele frequency: 3.692762186115214e-5
allele num: 27080
alternate allele: CGGAG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.479_480insGGAG
  hgvsp: ENSP00000361429.3:p.His161GlufsTer?
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.530_531insGGAG
  hgvsp: ENSP00000391998.3:p.His178GlufsTer?
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.479_480insGGAG
  hgvsp: ENSP00000361434.5:p.His161GlufsTer89
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.503_504insGGAG
  hgvsp: ENSP00000387435.3:p.His169GlufsTer89
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.503_504insGGAG
  hgvsp: ENSP00000436727.1:p.His169GlufsTer89
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11632
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9170
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11277
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29301
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1110
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His169GlufsTer89
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

1-44402281-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402281
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402281
    reference: chr 1
allele count: 2
allele frequency: 5.096060745044081e-5
allele num: 39246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.507G>A
  hgvsp: ENST00000372354.3:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.558G>A
  hgvsp: ENST00000438616.3:c.558G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.531G>A
  hgvsp: ENST00000498139.2:c.531G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.531G>A
  hgvsp: ENST00000414809.3:c.531G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.507G>A
  hgvsp: ENST00000372359.5:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28823
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8204
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1558
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1765
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10693
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1764
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu177Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

1-44402285-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402285
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402285
    reference: chr 1
allele count: 1
allele frequency: 2.450620006861736e-5
allele num: 40806
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.562G>A
  hgvsp: ENSP00000391998.3:p.Ala188Thr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.535G>A
  hgvsp: ENSP00000436727.1:p.Ala179Thr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.511G>A
  hgvsp: ENSP00000361434.5:p.Ala171Thr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.535G>A
  hgvsp: ENSP00000387435.3:p.Ala179Thr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.511G>A
  hgvsp: ENSP00000361429.3:p.Ala171Thr
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6051
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10815
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7922
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28353
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 809
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28542
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7742
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1934
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10940
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1355
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala179Thr
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-44402287-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402287
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402287
    reference: chr 1
allele count: 1
allele frequency: 2.420135527589545e-5
allele num: 41320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.564C>T
  hgvsp: ENST00000438616.3:c.564C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.513C>T
  hgvsp: ENST00000372354.3:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.537C>T
  hgvsp: ENST00000414809.3:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.513C>T
  hgvsp: ENST00000372359.5:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.537C>T
  hgvsp: ENST00000498139.2:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6458
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28066
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 10366
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 1.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 504
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 932
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 7698
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 540
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
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genotype quality: GenotypeQuality
  all individuals: 904
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genotype quality: GenotypeQuality
  all individuals: 3
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genotype quality: GenotypeQuality
  all individuals: 1
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genotype quality: GenotypeQuality
  all individuals: 1765
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genotype quality: GenotypeQuality
  all individuals: 342
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genotype quality: GenotypeQuality
  all individuals: 1072
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2046
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala179Ala
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

1-44402294-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402294
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402294
    reference: chr 1
allele count: 1
allele frequency: 2.277593039675671e-5
allele num: 43906
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.544C>T
  hgvsp: ENST00000498139.2:c.544C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.544C>T
  hgvsp: ENST00000414809.3:c.544C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.571C>T
  hgvsp: ENST00000438616.3:c.571C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.520C>T
  hgvsp: ENST00000372354.3:c.520C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.520C>T
  hgvsp: ENST00000372359.5:c.520C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7856
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
  all individuals: 1100
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 530
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 6
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu182Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/1-44402297-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402297
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402297
    reference: chr 1
allele count: 1
allele frequency: 2.25713253882268e-5
allele num: 44304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.523C>A
  hgvsp: ENST00000372354.3:c.523C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.523C>A
  hgvsp: ENST00000372359.5:c.523C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.547C>A
  hgvsp: ENST00000498139.2:c.547C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.547C>A
  hgvsp: ENST00000414809.3:c.547C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.574C>A
  hgvsp: ENST00000438616.3:c.574C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9052
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7945
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
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genotype depth: GenotypeDepth
  all individuals: 0
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1302
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2686
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26934
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 2529
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg183Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

1-44402299-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402299
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402299
    reference: chr 1
allele count: 1
allele frequency: 2.194426157559798e-5
allele num: 45570
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.525A>G
  hgvsp: ENST00000372359.5:c.525A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.576A>G
  hgvsp: ENST00000438616.3:c.576A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.525A>G
  hgvsp: ENST00000372354.3:c.525A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.549A>G
  hgvsp: ENST00000414809.3:c.549A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.549A>G
  hgvsp: ENST00000498139.2:c.549A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7721
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2743
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1227
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27906
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1677
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7748
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg183Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/1-44402301-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402301
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402301
    reference: chr 1
allele count: 1
allele frequency: 2.190868460257646e-5
allele num: 45644
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.578C>A
  hgvsp: ENSP00000391998.3:p.Pro193Gln
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.551C>A
  hgvsp: ENSP00000436727.1:p.Pro184Gln
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.527C>A
  hgvsp: ENSP00000361429.3:p.Pro176Gln
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.551C>A
  hgvsp: ENSP00000387435.3:p.Pro184Gln
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.527C>A
  hgvsp: ENSP00000361434.5:p.Pro176Gln
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8398
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4164
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7736
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27101
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2145
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1357
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8689
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2684
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27345
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1800
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro184Gln
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/1-44402303-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402303
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402303
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 45960
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.553C>A
  hgvsp: ENSP00000436727.1:p.Pro185Thr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.580C>A
  hgvsp: ENSP00000391998.3:p.Pro194Thr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.529C>A
  hgvsp: ENSP00000361434.5:p.Pro177Thr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.529C>A
  hgvsp: ENSP00000361429.3:p.Pro177Thr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.553C>A
  hgvsp: ENSP00000387435.3:p.Pro185Thr
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8815
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26759
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4696
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7708
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 690
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7851
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1539
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2993
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1979
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26329
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2829
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2774
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro185Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

1-44402303-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402303
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402303
    reference: chr 1
allele count: 6
allele frequency: 1.305483028720627e-4
allele num: 45960
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.529C>T
  hgvsp: ENSP00000361429.3:p.Pro177Ser
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.529C>T
  hgvsp: ENSP00000361434.5:p.Pro177Ser
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.580C>T
  hgvsp: ENSP00000391998.3:p.Pro194Ser
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.553C>T
  hgvsp: ENSP00000436727.1:p.Pro185Ser
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.553C>T
  hgvsp: ENSP00000387435.3:p.Pro185Ser
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4696
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8815
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7708
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7831
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2829
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7851
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26329
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1539
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2993
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro185Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum

http://identifiers.org/exac.variant/1-44402305-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402305
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402305
    reference: chr 1
allele count: 1
allele frequency: 2.138945927446954e-5
allele num: 46752
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.582C>A
  hgvsp: ENST00000438616.3:c.582C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.555C>A
  hgvsp: ENST00000414809.3:c.555C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.531C>A
  hgvsp: ENST00000372359.5:c.531C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.531C>A
  hgvsp: ENST00000372354.3:c.531C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.555C>A
  hgvsp: ENST00000498139.2:c.555C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8238
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4772
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8971
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26780
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7705
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genotype depth: GenotypeDepth
  all individuals: 10
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genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1521
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 21
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3142
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 2905
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2870
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7781
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 909
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2067
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7777
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro185Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

1-44402311-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402311
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402311
    reference: chr 1
allele count: 2
allele frequency: 4.114887663566784e-5
allele num: 48604
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.537C>T
  hgvsp: ENST00000372354.3:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.588C>T
  hgvsp: ENST00000438616.3:c.588C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.561C>T
  hgvsp: ENST00000498139.2:c.561C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.537C>T
  hgvsp: ENST00000372359.5:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.561C>T
  hgvsp: ENST00000414809.3:c.561C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26740
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5082
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8309
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7435
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genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2218
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8258
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 7582
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2263
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26987
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genotype quality: GenotypeQuality
  all individuals: 3285
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genotype quality: GenotypeQuality
  all individuals: 144
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genotype quality: GenotypeQuality
  all individuals: 22
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genotype quality: GenotypeQuality
  all individuals: 597
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genotype quality: GenotypeQuality
  all individuals: 1584
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly187Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD

1-44402318-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402318
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402318
    reference: chr 1
allele count: 1
allele frequency: 1.977848101265823e-5
allele num: 50560
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.544C>G
  hgvsp: ENSP00000361429.3:p.Pro182Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.595C>G
  hgvsp: ENSP00000391998.3:p.Pro199Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.568C>G
  hgvsp: ENSP00000436727.1:p.Pro190Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.568C>G
  hgvsp: ENSP00000387435.3:p.Pro190Ala
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.544C>G
  hgvsp: ENSP00000361434.5:p.Pro182Ala
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10087
  bin: 1.25e1
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genotype depth: GenotypeDepth
  all individuals: 6829
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5358
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 612
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genotype quality: GenotypeQuality
  all individuals: 1028
  bin: 4.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 572
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2406
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genotype quality: GenotypeQuality
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro190Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

1-44402330-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402330
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402330
    reference: chr 1
allele count: 1
allele frequency: 1.821759090577862e-5
allele num: 54892
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.556C>T
  hgvsp: ENSP00000361434.5:p.Pro186Ser
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.580C>T
  hgvsp: ENSP00000387435.3:p.Pro194Ser
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.607C>T
  hgvsp: ENSP00000391998.3:p.Pro203Ser
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.556C>T
  hgvsp: ENSP00000361429.3:p.Pro186Ser
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.580C>T
  hgvsp: ENSP00000436727.1:p.Pro194Ser
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5330
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genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5060
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10618
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1640
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27971
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10179
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3335
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2413
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3679
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5413
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro194Ser
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP

1-44402334-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402334
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402334
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 56716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.584G>A
  hgvsp: ENSP00000436727.1:p.Cys195Tyr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.560G>A
  hgvsp: ENSP00000361429.3:p.Cys187Tyr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.611G>A
  hgvsp: ENSP00000391998.3:p.Cys204Tyr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.584G>A
  hgvsp: ENSP00000387435.3:p.Cys195Tyr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.560G>A
  hgvsp: ENSP00000361434.5:p.Cys187Tyr
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10623
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4922
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4841
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26125
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2371
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11241
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 819
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3299
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3674
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27954
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4999
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
hgvs: p.Cys195Tyr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

1-44402335-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402335
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402335
    reference: chr 1
allele count: 1
allele frequency: 1.741978190433056e-5
allele num: 57406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.561C>T
  hgvsp: ENST00000372354.3:c.561C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.585C>T
  hgvsp: ENST00000414809.3:c.585C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.612C>T
  hgvsp: ENST00000438616.3:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.585C>T
  hgvsp: ENST00000498139.2:c.585C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.561C>T
  hgvsp: ENST00000372359.5:c.561C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4806
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10636
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26037
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4857
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1376
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27956
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genotype quality: GenotypeQuality
  all individuals: 11465
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 2
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 914
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Cys195Cys
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-44402339-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402339
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402339
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 58998
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.589C>A
  hgvsp: ENST00000414809.3:c.589C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.616C>A
  hgvsp: ENST00000438616.3:c.616C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.565C>A
  hgvsp: ENST00000372359.5:c.565C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.589C>A
  hgvsp: ENST00000498139.2:c.589C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.565C>A
  hgvsp: ENST00000372354.3:c.565C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 12245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10656
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25613
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4759
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3265
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4406
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2394
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 866
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3628
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 835
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 978
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11781
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg197Arg
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

1-44402344-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402344
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402344
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 61900
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.570C>T
  hgvsp: ENST00000372359.5:c.570C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.594C>T
  hgvsp: ENST00000414809.3:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.621C>T
  hgvsp: ENST00000438616.3:c.621C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.594C>T
  hgvsp: ENST00000498139.2:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.570C>T
  hgvsp: ENST00000372354.3:c.570C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3910
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24778
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4434
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 973
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2317
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3873
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3131
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Pro198Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/1-44402346-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402346
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402346
    reference: chr 1
allele count: 2
allele frequency: 3.178336458697518e-5
allele num: 62926
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.596C>A
  hgvsp: ENSP00000436727.1:p.Thr199Lys
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.623C>A
  hgvsp: ENSP00000391998.3:p.Thr208Lys
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.596C>A
  hgvsp: ENSP00000387435.3:p.Thr199Lys
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.572C>A
  hgvsp: ENSP00000361434.5:p.Thr191Lys
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.572C>A
  hgvsp: ENSP00000361429.3:p.Thr191Lys
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10340
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3763
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
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genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4271
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3415
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3768
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1037
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 304
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14692
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 28
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26933
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2271
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 869
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr199Lys
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

1-44402347-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402347
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402347
    reference: chr 1
allele count: 11
allele frequency: 1.734961042238415e-4
allele num: 63402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.573G>A
  hgvsp: ENST00000372359.5:c.573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.597G>A
  hgvsp: ENST00000414809.3:c.597G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.573G>A
  hgvsp: ENST00000372354.3:c.573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.624G>A
  hgvsp: ENST00000438616.3:c.624G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.597G>A
  hgvsp: ENST00000498139.2:c.597G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24284
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10299
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3740
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14794
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 222
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3077
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1396
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 866
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3672
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1064
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genotype quality: GenotypeQuality
  all individuals: 772
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26499
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genotype quality: GenotypeQuality
  all individuals: 601
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genotype quality: GenotypeQuality
  all individuals: 2288
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genotype quality: GenotypeQuality
  all individuals: 13887
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genotype quality: GenotypeQuality
  all individuals: 3419
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 947
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr199Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD

1-44402354-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402354
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402354
    reference: chr 1
allele count: 1
allele frequency: 1.460835013293599e-5
allele num: 68454
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.604G>C
  hgvsp: ENSP00000387435.3:p.Glu202Gln
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.580G>C
  hgvsp: ENSP00000361429.3:p.Glu194Gln
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.604G>C
  hgvsp: ENSP00000436727.1:p.Glu202Gln
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.631G>C
  hgvsp: ENSP00000391998.3:p.Glu211Gln
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.580G>C
  hgvsp: ENSP00000361434.5:p.Glu194Gln
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22489
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3487
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18835
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9269
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1042
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 671
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 2
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19071
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genotype quality: GenotypeQuality
  all individuals: 415
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 246
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2891
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 3
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genotype quality: GenotypeQuality
  all individuals: 664
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 3109
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu202Gln
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

1-44402357-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402357
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402357
    reference: chr 1
allele count: 1
allele frequency: 1.41759519151711e-5
allele num: 70542
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.583G>A
  hgvsp: ENSP00000361429.3:p.Ala195Thr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.607G>A
  hgvsp: ENSP00000387435.3:p.Ala203Thr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.607G>A
  hgvsp: ENSP00000436727.1:p.Ala203Thr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.634G>A
  hgvsp: ENSP00000391998.3:p.Ala212Thr
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.583G>A
  hgvsp: ENSP00000361434.5:p.Ala195Thr
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21789
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8739
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3106
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24659
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2406
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2682
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2901
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20916
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala203Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

1-44402371-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44402371
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 44402371
    reference: chr 1
allele count: 3
allele frequency: 3.822435146017022e-5
allele num: 78484
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000387435
  ensembl transcript: ENST00000414809
  gene symbol: ARTN
  hgvsc: ENST00000414809.3:c.621G>C
  hgvsp: ENSP00000387435.3:p.Met207Ile
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361429
  ensembl transcript: ENST00000372354
  gene symbol: ARTN
  hgvsc: ENST00000372354.3:c.597G>C
  hgvsp: ENSP00000361429.3:p.Met199Ile
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000391998
  ensembl transcript: ENST00000438616
  gene symbol: ARTN
  hgvsc: ENST00000438616.3:c.648G>C
  hgvsp: ENSP00000391998.3:p.Met216Ile
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000361434
  ensembl transcript: ENST00000372359
  gene symbol: ARTN
  hgvsc: ENST00000372359.5:c.597G>C
  hgvsp: ENSP00000361434.5:p.Met199Ile
  variant of: http://identifiers.org/hgnc/727
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000117407
  ensembl protein: ENSP00000436727
  ensembl transcript: ENST00000498139
  gene symbol: ARTN
  hgvsc: ENST00000498139.2:c.621G>C
  hgvsp: ENSP00000436727.1:p.Met207Ile
  variant of: http://identifiers.org/hgnc/727
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25984
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7073
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Met207Ile
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 402
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45339
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7039
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3546
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60150
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8100
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4988
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8202
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.955070246209486e-5
allele num: 14378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10442
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.38e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.266445e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.94e-1

QD
type: SiteQuality
SIO_000300: 1.024e1

GenotypeQuality
all individuals: 94
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6061
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3737
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46204
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8268
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.633026324384349e-5
allele num: 61236
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8288
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5204
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10676
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.22e0

FS
type: SiteQuality
SIO_000300: 2.062e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.42e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.818e0

MQ
type: SiteQuality
SIO_000300: 5.896e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.288257e6

QD
type: SiteQuality
SIO_000300: 8.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.27e-1

GenotypeQuality
all individuals: 439
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47192
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3842
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5398
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8350
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14888
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10794
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.613423685059697e-5
allele num: 61980
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: -1.796e0

FS
type: SiteQuality
SIO_000300: 1.461e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.7e-2

MQ
type: SiteQuality
SIO_000300: 5.939e1

DP
type: SiteQuality
SIO_000300: 1.30376e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.094e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.9e-1

QD
type: SiteQuality
SIO_000300: 4.72e0

GenotypeQuality
all individuals: 3805
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47158
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5317
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 661
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 495
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62170
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.562099263832819e-4
allele num: 8422
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10846
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8358
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14960
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.035e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.306799e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.76e-1

FS
type: SiteQuality
SIO_000300: 1.498e0

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.04e-1

GenotypeQuality
all individuals: 13
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5248
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47390
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3807
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62276
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14990
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8360
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10858
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5420
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.95e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.251e1

VQSLOD
type: SiteQuality
SIO_000300: -1.887e0

FS
type: SiteQuality
SIO_000300: 5.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

DP
type: SiteQuality
SIO_000300: 1.308491e6

GenotypeQuality
all individuals: 16
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 391
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47840
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.197748784855462e-5
allele num: 62544
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 9.145783793671118e-5
allele num: 10934
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

QD
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SIO_000300: 1.16e1

BaseQRankSum
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SIO_000300: -7.32e-1

ReadPosRankSum
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SIO_000300: 5.02e-1

MQRankSum
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VQSLOD
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ClippingRankSum
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SIO_000300: -9.71e-1

FS
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SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -8.0e-4

DP
type: SiteQuality
SIO_000300: 1.314742e6

MQ
type: SiteQuality
SIO_000300: 5.922e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10952
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.599027791103009e-5
allele num: 62538
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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ReadPosRankSum
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SIO_000300: 8.35e-1

FS
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MQRankSum
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DP
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MQ
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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SIO_000300: -1.429e0

InbreedingCoeff
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SIO_000300: -1.3e-3

QD
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
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allele num: 62392
num of homozygotes: 0

Other
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African
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allele count: 4
allele frequency: 4.69593801361822e-4
allele num: 8518
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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InbreedingCoeff
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DP
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VQSLOD
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ClippingRankSum
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MQ
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QD
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FS
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SIO_000300: 5.372e0

BaseQRankSum
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MQRankSum
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SIO_000300: 9.1e-1

ReadPosRankSum
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SIO_000300: 2.96e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62202
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.147457006952067e-5
allele num: 10932
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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ReadPosRankSum
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SIO_000300: 1.03e-1

ClippingRankSum
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MQRankSum
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InbreedingCoeff
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FS
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DP
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MQ
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SIO_000300: 6.0e1

QD
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BaseQRankSum
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SIO_000300: -7.42e-1

VQSLOD
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5410
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 10896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8296
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.234361860404942e-5
allele num: 61836
num of homozygotes: 0

African
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num of homozygotes: 0

South Asian
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e0

FS
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InbreedingCoeff
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MQRankSum
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DP
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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MQ
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8332
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 5386
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15072
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61688
num of homozygotes: 0

Other
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 1.840942562592047e-4
allele num: 10864
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ClippingRankSum
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VQSLOD
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MQRankSum
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DP
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MQ
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FS
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 768
num of homozygotes: 0

Latino
type: Population
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allele frequency: 9.281603861147207e-5
allele num: 10774
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

East Asian
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South Asian
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African
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European (Non-Finnish)
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MQ
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQRankSum
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DP
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 465
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8050
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10704
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8210
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5278
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.649402916144356e-5
allele num: 60628
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

DP
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SIO_000300: 1.258266e6

QD
type: SiteQuality
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FS
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SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

MQRankSum
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SIO_000300: -1.38e0

MQ
type: SiteQuality
SIO_000300: 5.056e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 1009
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7690
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8038
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.840881105486387e-5
allele num: 14618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58692
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5056
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10482
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

VQSLOD
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QD
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SIO_000300: 5.35e0

ClippingRankSum
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SIO_000300: 4.74e-1

MQRankSum
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SIO_000300: 4.74e-1

ReadPosRankSum
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DP
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SIO_000300: 1.210323e6

FS
type: SiteQuality
SIO_000300: 2.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 42

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

Other
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allele frequency: 1.36986301369863e-3
allele num: 730
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 58246
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14576
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5026
num of homozygotes: 0

Latino
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allele frequency: 9.595087315294569e-5
allele num: 10422
num of homozygotes: 0

African
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allele count: 41
allele frequency: 5.356676247713614e-3
allele num: 7654
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.57e-1

MQ
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SIO_000300: 6.0e1

QD
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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DP
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SIO_000300: 1.201077e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.06e-1

FS
type: SiteQuality
SIO_000300: 1.344e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 712
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14328
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 56888
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.344809037116729e-4
allele num: 7436
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.717e0

QD
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SIO_000300: 1.299e1

MQRankSum
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SIO_000300: -1.46e-1

ReadPosRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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SIO_000300: -7.45e-1

VQSLOD
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SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-2

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 11

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 137
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7362
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 706
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 56308
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4842
num of homozygotes: 0

South Asian
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allele frequency: 7.724719101123596e-4
allele num: 14240
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7798
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-3

DP
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VQSLOD
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FS
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MQ
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: 1.07e0

QD
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SIO_000300: 1.128e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 707
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4606
num of homozygotes: 0

Latino
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allele frequency: 1.025851456709069e-4
allele num: 9748
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 53640
num of homozygotes: 0

Other
type: Population
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MQ
type: SiteQuality
SIO_000300: 5.941e1

InbreedingCoeff
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VQSLOD
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ClippingRankSum
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QD
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MQRankSum
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ReadPosRankSum
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FS
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 5876
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 2.589331952356292e-4
allele num: 3862
num of homozygotes: 0

Other
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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VQSLOD
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MQRankSum
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QD
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DP
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8140
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.221136333348141e-5
allele num: 45022
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European (Finnish)
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allele frequency: 0.0e0
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Other
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BaseQRankSum
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SIO_000300: -9.73e-1

QD
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InbreedingCoeff
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SIO_000300: -1.2e-2

VQSLOD
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SIO_000300: 5.56e-1

FS
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ClippingRankSum
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SIO_000300: 9.73e-1

ReadPosRankSum
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SIO_000300: -5.84e-1

MQRankSum
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SIO_000300: -1.17e-1

DP
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SIO_000300: 8.48067e5

MQ
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SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 7.422068283028204e-4
allele num: 8084
num of homozygotes: 0

ClippingRankSum
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SIO_000300: 2.7e-2

QD
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ReadPosRankSum
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FS
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MQRankSum
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DP
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BaseQRankSum
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VQSLOD
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SIO_000300: 1.13e0

MQ
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InbreedingCoeff
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SIO_000300: -1.24e-2

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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num of homozygotes: 0

African
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South Asian
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Latino
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allele frequency: 1.321003963011889e-4
allele num: 7570
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
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DP
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InbreedingCoeff
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QD
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FS
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MQ
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MQRankSum
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: 4.72e-1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.468526289804987e-5
allele num: 40510
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3336
num of homozygotes: 0

Other
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MQRankSum
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SIO_000300: 1.55e0

VQSLOD
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FS
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QD
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ReadPosRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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SIO_000300: -1.67e-2

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 40

African
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allele frequency: 2.382086707956169e-4
allele num: 4198
num of homozygotes: 0

Latino
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allele frequency: 4.733354370463869e-4
allele num: 6338
num of homozygotes: 0

European (Non-Finnish)
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allele count: 37
allele frequency: 1.089837997054492e-3
allele num: 33950
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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Other
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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MQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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FS
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InbreedingCoeff
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele num: 4480
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East Asian
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African
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South Asian
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European (Non-Finnish)
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ReadPosRankSum
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FS
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QD
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VQSLOD
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
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East Asian
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African
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South Asian
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European (Non-Finnish)
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ReadPosRankSum
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BaseQRankSum
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QD
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VQSLOD
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ClippingRankSum
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FS
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InbreedingCoeff
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MQRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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num of homozygotes: 0

East Asian
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South Asian
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European (Finnish)
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Other
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BaseQRankSum
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ReadPosRankSum
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MQ
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QD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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VQSLOD
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FS
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DP
type: SiteQuality
SIO_000300: 3.17248e5

GenotypeDepth
all individuals: 818
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1980
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 3.25e1
variant carriers: 5

GenotypeQuality
all individuals: 762
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5534
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 128
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 10875
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 168
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 0
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2541
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 24430
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 157
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 2.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 7.194244604316547e-3
allele num: 278
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 1.5625e-2
allele num: 256
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.968641114982578e-4
allele num: 2870
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.496503496503497e-3
allele num: 286
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 7.541478129713424e-4
allele num: 5304
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 108
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.386e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.034e-1

FS
type: SiteQuality
SIO_000300: 2.1386e1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.89e-1

DP
type: SiteQuality
SIO_000300: 2.6844e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

QD
type: SiteQuality
SIO_000300: 9.0e-1

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3681
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 69
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variant carriers: 0

GenotypeQuality
all individuals: 1788
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2132
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8588
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1340
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28714
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 9.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 396
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 478
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 104
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6084
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3790
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.779999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -1.649e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.89e-2

DP
type: SiteQuality
SIO_000300: 2.64169e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.38e0

MQ
type: SiteQuality
SIO_000300: 5.728e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2536
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26443
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 267
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variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 736
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5851
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 184
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3400
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 216
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 98
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1488
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.78e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 1.60329e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.95e-1

QD
type: SiteQuality
SIO_000300: 9.08e0

GenotypeDepth
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 811
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26395
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2302
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5293
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1222
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2980
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 146
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 90
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -9.177e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.88e-2

QD
type: SiteQuality
SIO_000300: 3.26e0

FS
type: SiteQuality
SIO_000300: 9.699999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.22e-1

DP
type: SiteQuality
SIO_000300: 1.46805e5

GenotypeQuality
all individuals: 3542
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 349
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variant carriers: 0

GenotypeQuality
all individuals: 317
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variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 1

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.470588235294118e-2
allele num: 68
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 358
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.522e0

VQSLOD
type: SiteQuality
SIO_000300: -8.396e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

QD
type: SiteQuality
SIO_000300: 1.213e1

MQRankSum
type: SiteQuality
SIO_000300: 6.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.76e-1

DP
type: SiteQuality
SIO_000300: 5.6149e4

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.058e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.7e-1

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 1

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 191
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.057e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 5.0786e4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

QD
type: SiteQuality
SIO_000300: 1.447e1

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 14902
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 80
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.236e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 4.3241e4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.038e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.524e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

GenotypeQuality
all individuals: 220
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1925
bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.015e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 4.2714e4

VQSLOD
type: SiteQuality
SIO_000300: -2.142e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.026e0

GenotypeQuality
all individuals: 14665
bin: 7.5e0
variant carriers: 6

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 2

GenotypeQuality
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bin: 1.25e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 4.1129e4

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.015e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.656e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeQuality
all individuals: 4
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3
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variant carriers: 3

GenotypeQuality
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bin: 4.25e1
variant carriers: 2

GenotypeQuality
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variant carriers: 23

GenotypeQuality
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variant carriers: 72

GenotypeQuality
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variant carriers: 26

GenotypeQuality
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bin: 2.25e1
variant carriers: 21

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 7

GenotypeQuality
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variant carriers: 6

GenotypeQuality
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variant carriers: 8

GenotypeQuality
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variant carriers: 22

GenotypeQuality
all individuals: 12
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variant carriers: 12

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 4

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 5.0e-1
allele num: 6
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 2.142857142857143e-1
allele num: 14
num of homozygotes: 0

South Asian
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allele count: 5
allele frequency: 8.064516129032258e-2
allele num: 62
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.785e0

VQSLOD
type: SiteQuality
SIO_000300: 2.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 4.0023e4

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.46e-2

QD
type: SiteQuality
SIO_000300: 1.42e1

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 7.66e0

VQSLOD
type: SiteQuality
SIO_000300: 4.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 3.1245e4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeQuality
all individuals: 823
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 58
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.082e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.8777e4

VQSLOD
type: SiteQuality
SIO_000300: 1.45e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.760000000000001e-2

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.68e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.4429e4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.502e1

VQSLOD
type: SiteQuality
SIO_000300: 2.12e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.91e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.072e-1

QD
type: SiteQuality
SIO_000300: 1.598e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 1.8881e4

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 6.587615283267457e-4
allele num: 4554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 106
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1352
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.75618e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

FS
type: SiteQuality
SIO_000300: 1.951e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.48e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -8.459999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.48e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 120
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5142
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1608
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.19047619047619e-2
allele num: 84
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e0

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.96147e5

QD
type: SiteQuality
SIO_000300: 1.6e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.573e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.19e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.88e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -3.044e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 503
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 96
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 142
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2088
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5882
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.25e0

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.580000000000001e-2

DP
type: SiteQuality
SIO_000300: 2.29893e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 1.545e1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
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GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

European (Finnish)
type: Population
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allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 244
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 264
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6686
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2792
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

QD
type: SiteQuality
SIO_000300: 2.55e0

MQ
type: SiteQuality
SIO_000300: 4.41e1

MQRankSum
type: SiteQuality
SIO_000300: -1.231e0

VQSLOD
type: SiteQuality
SIO_000300: 7.199999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 2.83227e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6516
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variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 232
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1382
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.281065846784525e-4
allele num: 7806
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7840
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.25276e5

MQRankSum
type: SiteQuality
SIO_000300: -1.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.16e0

MQ
type: SiteQuality
SIO_000300: 6.026e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.25e-1

QD
type: SiteQuality
SIO_000300: 1.309e1

FS
type: SiteQuality
SIO_000300: 2.632e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.408e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.57e-2

GenotypeQuality
all individuals: 774
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 558
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 364
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 972
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8454
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 4.170141784820684e-4
allele num: 2398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.5e-3
allele num: 400
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.624431448992852e-4
allele num: 12312
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.05955e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.96e-1

QD
type: SiteQuality
SIO_000300: 7.73e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.39e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.93e0

GenotypeQuality
all individuals: 774
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1398
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.182872013248167e-4
allele num: 8454
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 972
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12312
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.93e0

QD
type: SiteQuality
SIO_000300: 7.73e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.39e-2

DP
type: SiteQuality
SIO_000300: 5.05955e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 147
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12866
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2530
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1048
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.17343346632246e-4
allele num: 8522
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e-2

FS
type: SiteQuality
SIO_000300: 3.255e0

QD
type: SiteQuality
SIO_000300: 9.699999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e-1

MQ
type: SiteQuality
SIO_000300: 5.689e1

DP
type: SiteQuality
SIO_000300: 5.15287e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.63e-2

MQRankSum
type: SiteQuality
SIO_000300: -8.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.76e-1

GenotypeQuality
all individuals: 7979
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28535
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 843
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 2
allele frequency: 2.122241086587436e-4
allele num: 9424
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1038
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4114
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20004
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1874
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.94e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

FS
type: SiteQuality
SIO_000300: 5.97e0

DP
type: SiteQuality
SIO_000300: 6.05555e5

VQSLOD
type: SiteQuality
SIO_000300: -5.534e-1

QD
type: SiteQuality
SIO_000300: 1.001e1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

GenotypeQuality
all individuals: 1908
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 1

GenotypeQuality
all individuals: 23
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4274
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2628
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1984
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.783773440489859e-5
allele num: 20904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1144
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.42e-1

QD
type: SiteQuality
SIO_000300: 5.75e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.93e-2

DP
type: SiteQuality
SIO_000300: 6.14613e5

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.275e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

GenotypeQuality
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27952
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 664
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variant carriers: 0

GenotypeQuality
all individuals: 2114
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 300
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2036
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.721435316336166e-5
allele num: 21180
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4344
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2662
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.606e1

DP
type: SiteQuality
SIO_000300: 6.16435e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.97e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.211e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.69e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.938e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.73e-1

GenotypeQuality
all individuals: 28056
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variant carriers: 0

GenotypeQuality
all individuals: 54
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variant carriers: 0

GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
all individuals: 1414
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GenotypeQuality
all individuals: 507
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GenotypeQuality
all individuals: 21
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1334
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.397924179787141e-5
allele num: 22738
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2224
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 318
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4602
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2920
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 6.2568e5

ClippingRankSum
type: SiteQuality
SIO_000300: 9.88e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.939e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.8e-1

FS
type: SiteQuality
SIO_000300: 1.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.96e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.909e1

GenotypeQuality
all individuals: 669
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
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variant carriers: 0

GenotypeQuality
all individuals: 8584
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GenotypeQuality
all individuals: 1652
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variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22968
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2250
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 318
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.362474781439139e-4
allele num: 2974
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4644
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.05e-2

DP
type: SiteQuality
SIO_000300: 6.26479e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.22e-1

FS
type: SiteQuality
SIO_000300: 5.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9395
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GenotypeQuality
all individuals: 2592
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 324
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23784
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2314
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4792
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3052
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.01010101010101e-4
allele num: 9900
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -6.679e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.591e0

QD
type: SiteQuality
SIO_000300: 8.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.92e-2

DP
type: SiteQuality
SIO_000300: 6.30991e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 511
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variant carriers: 0

GenotypeQuality
all individuals: 7834
bin: 7.5e0
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4806
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 326
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.287310979618672e-4
allele num: 3042
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2332
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9898
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23782
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.829e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

FS
type: SiteQuality
SIO_000300: 1.711e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -2.829e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.95e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.97e-1

QD
type: SiteQuality
SIO_000300: 8.8e-1

DP
type: SiteQuality
SIO_000300: 6.31554e5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 7831
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 19
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3046
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23998
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2376
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4822
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1498
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 326
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

FS
type: SiteQuality
SIO_000300: 8.88e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.92e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.74e-1

DP
type: SiteQuality
SIO_000300: 6.33775e5

QD
type: SiteQuality
SIO_000300: 1.086e1

GenotypeQuality
all individuals: 879
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2774
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1979
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3046
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1498
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 6.064281382656155e-4
allele num: 9894
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4822
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2376
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23998
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.92e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.55e-1

FS
type: SiteQuality
SIO_000300: 8.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-2

DP
type: SiteQuality
SIO_000300: 6.33775e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.74e-1

QD
type: SiteQuality
SIO_000300: 1.086e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-2

GenotypeQuality
all individuals: 80
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26352
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.00341159943809e-4
allele num: 9966
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 332
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2396
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3116
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4890
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.67e0

FS
type: SiteQuality
SIO_000300: 7.025e0

DP
type: SiteQuality
SIO_000300: 6.35462e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.97e-2

QD
type: SiteQuality
SIO_000300: 9.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.49e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.2e-1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3084
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 934
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 7.804573480059315e-5
allele num: 25626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5090
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10092
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1598
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3304
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.361e0

MQRankSum
type: SiteQuality
SIO_000300: 7.01e-1

DP
type: SiteQuality
SIO_000300: 6.44426e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.94e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.316e0

FS
type: SiteQuality
SIO_000300: 1.673e1

MQ
type: SiteQuality
SIO_000300: 5.925e1

QD
type: SiteQuality
SIO_000300: 1.813e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2251
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8188
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3480
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1730
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10160
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2750
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5258
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.728004771846108e-5
allele num: 26824
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.294e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.066e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.11e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.62e0

VQSLOD
type: SiteQuality
SIO_000300: -9.367e-1

DP
type: SiteQuality
SIO_000300: 6.57207e5

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.78e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 8
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 630
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 93
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variant carriers: 0

GenotypeQuality
all individuals: 901
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3158
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5616
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1974
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.583979328165374e-4
allele num: 3870
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.79e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.148e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.46e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.453e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.45e0

MQRankSum
type: SiteQuality
SIO_000300: -6.76e-1

MQ
type: SiteQuality
SIO_000300: 5.766e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.05e0

DP
type: SiteQuality
SIO_000300: 6.96e5

GenotypeQuality
all individuals: 624
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 1409
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 903
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variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2080
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4040
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30640
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5818
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 396
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10450
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.26e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.32e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.89e-1

QD
type: SiteQuality
SIO_000300: 1.138e1

DP
type: SiteQuality
SIO_000300: 7.12712e5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2415
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 287
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 2.969121140142518e-4
allele num: 3368
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2112
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4110
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5914
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31014
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-2

QD
type: SiteQuality
SIO_000300: 1.057e1

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.641e0

DP
type: SiteQuality
SIO_000300: 7.16605e5

VQSLOD
type: SiteQuality
SIO_000300: -9.339e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e0

FS
type: SiteQuality
SIO_000300: 8.734999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.333e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6078
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4280
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3498
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2226
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31986
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.21e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 7.32429e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.831e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4500
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2400
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3772
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33716
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10672
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 4.834e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.307e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

MQ
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.12e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4604
num of homozygotes: 0

Latino
type: Population
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allele frequency: 1.530924678505818e-4
allele num: 6532
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.912904165452957e-5
allele num: 34330
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 434
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3856
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.246e0

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-2

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 7.72822e5

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.97e-1

VQSLOD
type: SiteQuality
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GenotypeQuality
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variant carriers: 10

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 26
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GenotypeQuality
all individuals: 119
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variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2498
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Other
type: Population
allele count: 1
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allele num: 440
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South Asian
type: Population
allele count: 6
allele frequency: 5.598059339428998e-4
allele num: 10718
num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.156002543205595e-4
allele num: 34602
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.89e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.02e-2

DP
type: SiteQuality
SIO_000300: 7.75606e5

FS
type: SiteQuality
SIO_000300: 1.768e0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

QD
type: SiteQuality
SIO_000300: 1.43e1

GenotypeQuality
all individuals: 76
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1888
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5128
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2782
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7220
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.670512204240773e-5
allele num: 37446
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11012
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.68e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.999999999999999e-3

QD
type: SiteQuality
SIO_000300: 1.101e1

DP
type: SiteQuality
SIO_000300: 8.32025e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

GenotypeQuality
all individuals: 1734
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1111
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 751
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 88
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11166
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5328
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4568
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2854
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 478
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.587589918749676e-5
allele num: 38646
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.500000000000001e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.123e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.559e-1

MQ
type: SiteQuality
SIO_000300: 5.388e1

DP
type: SiteQuality
SIO_000300: 8.52873e5

QD
type: SiteQuality
SIO_000300: 1.232e1